Abstract
T cells genetically targeted with a chimeric antigen receptor (CAR) to B-cell malignancies have demonstrated tremendous clinical outcomes. With the proof in principle for CAR T cells as a therapy for B-cell malignancies being established, current and future research is being focused on adapting CAR technology to other cancers, as well as enhancing its efficacy and/or safety. The modular nature of the CAR, extracellular antigen-binding domain fused to a transmembrane domain and intracellular T-cell signaling domains, allows for optimization by replacement of the various components. These modifications are creating a whole new class of therapeutic CARs. In this review, we discuss the recent major advances in CAR design and how these modifications will impact its clinical application.
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CITATION STYLE
Abate-Daga, D., & Davila, M. L. (2016, May 18). CAR models: Next-generation CAR modifications for enhanced T-cell function. Molecular Therapy Oncolytics. Nature Publishing Group. https://doi.org/10.1038/mto.2016.14
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